Pure Global

Dextran-based Priming vs. Crystalloid and Mannitol-based Priming Solution in Adult Cardiac Surgery - Trial NCT02767154

Access comprehensive clinical trial information for NCT02767154 through Pure Global AI's free database. This Phase 2 trial is sponsored by Sahlgrenska University Hospital, Sweden and is currently Completed. The study focuses on Heart Disease. Target enrollment is 84 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

Free Database
Powered by Pure Global AI
840K+ Trials
Device Trial
NCT02767154
Phase 2
Completed
Device Trial
device
Trial Details
ClinicalTrials.gov โ€ข NCT02767154
View on ClinicalTrials.gov
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Dextran-based Priming vs. Crystalloid and Mannitol-based Priming Solution in Adult Cardiac Surgery
A Randomized Controlled Trial Comparing Dextran-based Priming (PrimECC), and Standard Crystalloid and Mannitol-based Priming Solution in Adult Cardiac Surgery

Study Focus

Heart Disease

A colloid Dextran 40 solution for extracorporeal circulation

Interventional

device

Sponsor & Location

Sahlgrenska University Hospital, Sweden

Gothenburg, Sweden

Timeline & Enrollment

Phase 2

May 01, 2016

Jul 13, 2017

84 participants

Primary Outcome

Change in oncotic pressure in plasma

Summary

This study will compare two priming solutions for extracorporeal circulation, one based on
 Dextran 40, one based on crystalloid and mannitol. Primary endpoint is oncotic pressure
 during cardiopulmonary bypass. Secondary endpoints included fluid balance and organ
 functions.

ICD-10 Classifications

Heart disease, unspecified
Complications and ill-defined descriptions of heart disease
Other ill-defined heart diseases
Other forms of heart disease
Hypertensive heart disease

Data Source

ClinicalTrials.gov

NCT02767154

Device Trial